ZOHAR TOOTHPASTE COOL MINT- sodium monofluorophosphate paste, dentifrice United States - English - NLM (National Library of Medicine)

zohar toothpaste cool mint- sodium monofluorophosphate paste, dentifrice

broom lane enterprises - sodium monofluorphosphate 1.15% (1500 ppm/ 0.15% w/v fluoride ion) - anticavity aids in the prevention of dental cavities

ZOHAR TOOTHPASTE REGULAR MINT- sodium monofluorophosphate paste, dentifrice United States - English - NLM (National Library of Medicine)

zohar toothpaste regular mint- sodium monofluorophosphate paste, dentifrice

broom lane enterprises - sodium monofluorphosphate 1.15% (1500 ppm/ 0.15% w/v fluoride ion) - anticavity aids in the prevention of dental cavities

SODIUM POLYSTYRENE SULFONATE powder United States - English - NLM (National Library of Medicine)

sodium polystyrene sulfonate powder

kvk-tech, inc. - sodium polystyrene sulfonate (unii: 1699g8679z) (polystyrene sulfonic acid - unii:70ko0r01ry) - sodium polystyrene sulfonate 1 g in 1 g - sodium polystyrene sulfonate is indicated for the treatment of hyperkalemia. limitation of use : sodium polystyrene sulfonate should not be used as an emergency treatment for life-threatening hyperkalemia because of its delayed onset of action [see clinical pharmacology (12.2)]. sodium polystyrene sulfonate is contraindicated in patients with the following conditions: • hypersensitivity to polystyrene sulfonate resins • obstructive bowel disease • neonates with reduced gut motility risk summary sodium polystyrene sulfonate is not absorbed systemically following oral or rectal administration and maternal use is not expected to result in fetal risk. risk summary sodium polystyrene sulfonate is not absorbed systemically by the mother, so breastfeeding is not expected to result in risk to the infant. studies of safety and efficacy have not been conducted in pediatric patients. in pediatric patients, as in adults, sodium polystyrene sulfonate is expected to bind potassium at the practical exchange ratio of 1 meq potassium per 1 gram of resin. in neonates, sodium polystyrene sulfonate should not be given by the oral route. in both children and neonates, excessive dosage or inadequate dilution could result in impaction of the resin. premature infants or low birth weight infants may have an increased risk for gastrointestinal adverse effects with sodium polystyrene sulfonate use [see warnings and precautions (5.4)] .

SODIUM POLYSTYRENE SULFONATE powder, for suspension United States - English - NLM (National Library of Medicine)

sodium polystyrene sulfonate powder, for suspension

sunrise pharmaceutical, inc. - sodium polystyrene sulfonate (unii: 1699g8679z) (polystyrene sulfonic acid - unii:70ko0r01ry) - sodium cation 4.1 meq in 1 g - sodium polystyrene sulfonate for suspension is indicated for the treatment of hyperkalemia. limitation of use : sodium polystyrene sulfonate for suspension should not be used as an emergency treatment for life-threatening hyperkalemia because of its delayed onset of action [see clinical pharmacology (12.2) ] sodium polystyrene sulfonate is contraindicated in patients with the following conditions: - hypersensitivity to polystyrene sulfonate resins - obstructive bowel disease - neonates with reduced gut motility risk summary sodium polystyrene sulfonate is not absorbed systemically following oral or rectal administration and maternal use is not expected to result in fetal risk. risk summary sodium polystyrene sulfonate is not absorbed systemically by the mother, so breastfeeding is not expected to result in risk to the infant. studies of safety and efficacy have not been conducted in pediatric patients. in pediatric patients, as in adults, sodium polystyrene sulfonate is expected to bind potassium at the pract

SODIUM CHLORIDE 0.9 % INTRAVENOUS INFUSION BP Israel - English - Ministry of Health

sodium chloride 0.9 % intravenous infusion bp

teva medical marketing ltd. - sodium chloride - solution for infusion - sodium chloride 0.9 %w/v - sodium chloride - sodium chloride - treatment of isotonic extracellular dehydration. treatment of sodium depletion. vehicle or diluent of compatible drugs for parenteral administration.

SODIUM CHLORIDE 0.9 % INTRAVENOUS INFUSION BP Israel - English - Ministry of Health

sodium chloride 0.9 % intravenous infusion bp

teva medical marketing ltd. - sodium chloride - solution for infusion - sodium chloride 0.9 %w/v - sodium chloride - sodium chloride - treatment of isotonic extracellular dehydration. treatment of sodium depletion. vehicle or diluent of compatible drugs for parenteral administration.

SF- 1.1% sodium fluoride gel United States - English - NLM (National Library of Medicine)

sf- 1.1% sodium fluoride gel

cypress pharmaceutical, inc. - sodium fluoride (unii: 8zyq1474w7) (fluoride ion - unii:q80vpu408o) - fluoride ion 11 mg in 1 g - a dental caries preventive, for once daily self-applied topical use.  it is well established that 1.1% sodium fluoride is safe and extraordinarily effective as a caries preventive when applied frequently with mouthpiece applicators.1-4 sf 1.1% brush-on gel in a squeeze-tube is easily applied onto a toothbrush as well as a mouthpiece tray.  this prescription dental gel should be used once daily following use of a regular toothpaste unless otherwise instructed by your dental professional.  may be used whether or not drinking water is fluoridated since topical fluoride cannot produce fluorosis. (see warnings for exception.) do not use in pediatric patients under age 6 years unless recommended by a dentist or physician. the use of sf 1.1% brush-on gel in pediatric age groups 6 to 16 years as a caries preventive is supported by pioneering clinical studies with 1.1% sodium fluoride gels in mouth trays in students age 11-14 years conducted by englander, et al.2,3,4 .  safety and effectiveness in pediatric patients

NAPROXEN SODIUM- naproxen sodium tablet United States - English - NLM (National Library of Medicine)

naproxen sodium- naproxen sodium tablet

lake erie medical dba quality care products llc - naproxen sodium (unii: 9tn87s3a3c) (naproxen - unii:57y76r9atq) - naproxen sodium 550 mg - carefully consider the potential benefits and risks of naproxen sodium tablets, usp and other treatment options before deciding to use naproxen sodium tablets, usp. use the lowest effective dose for the shortest duration consistent with individual patient treatment goals (see warnings ). naproxen, usp as naproxen sodium tablets, usp are indicated: - for the relief of the signs and symptoms of rheumatoid arthritis - for the relief of the signs and symptoms of osteoarthritis - for the relief of the signs and symptoms of ankylosing spondylitis - for the relief of the signs and symptoms of juvenile arthritis - for relief of the signs and symptoms of tendonitis - for relief of the signs and symptoms of bursitis - for relief of the signs and symptoms of acute gout - for the management of pain - for the management of primary dysmenorrhea naproxen sodium tablets, usp are contraindicated in patients with known hypersensitivity to naproxen, usp and naproxen sodium, usp. naproxen sodium, usp should not be given to patie

ANTICAVITY FLUORIDE- sodium fluoride mouthwash United States - English - NLM (National Library of Medicine)

anticavity fluoride- sodium fluoride mouthwash

ranir llc - sodium fluoride (unii: 8zyq1474w7) (fluoride ion - unii:q80vpu408o) - fluoride ion 0.1 mg in 1 ml - anticavity fluoride mouthwash aids in the prevention of dental cavities

SF 5000 PLUS- 1.1% sodium fluoride prescription dental cream cream United States - English - NLM (National Library of Medicine)

sf 5000 plus- 1.1% sodium fluoride prescription dental cream cream

cypress pharmaceutical, inc. - sodium fluoride (unii: 8zyq1474w7) (fluoride ion - unii:q80vpu408o) - fluoride ion 5 mg in 1 g - a dental caries preventive; for once daily self-applied topical use.  it is well established that 1.1% sodium fluoride is safe and extraordinarily effective as a caries preventive when applied frequently with mouthpiece applicators.1-4 sf 5000 plus brand of 1.1% sodium fluoride in a squeeze-tube is easily applied onto a toothbrush.  this prescription dental cream should be used once daily in place of your regular toothpaste unless otherwise instructed by your dental professional.  may be used whether or not drinking water is fluoridated, since topical fluoride cannot produce fluorosis. (see warnings for exception.) do not use in pediatric patients under age 6 years unless recommended by a dentist or physician.  the use of sf 5000 plus in pediatric age groups 6 to 16 years as a caries preventive is supported by pioneering clinical studies with 1.1% sodium fluoride gels in mouth trays in students age 11- 14 years conducted by englander, et al.2,3,4 safety and effectiveness in pediatric patients below the age